(Q31388417)

1 July 2017

title

Copper transport and its defect in Wilson disease: characterization of the copper-binding domain of Wilson disease ATPase (English)

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1 July 2017

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Sarkar B

1

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1 July 2017

publication date

1 April 2000

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Journal of Inorganic Biochemistry

1 July 2017

published in

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1 July 2017

volume

79

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1 July 2017

issue

1-4

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1 July 2017

page(s)

187-191

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Copper transport and its alterations in Menkes and Wilson diseases.

1 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

Isolation of a partial candidate gene for Menkes disease by positional cloning

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

The copper chaperone for superoxide dismutase

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Isolation of a cDNA encoding the human homolog of COX17, a yeast gene essential for mitochondrial copper recruitment

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7 January 2021

Characterization of a novel, membrane-bound, 80-kDa matrix-degrading protease from human breast cancer cells. Monoclonal antibody production, isolation, and localization

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7 January 2021

Evidence for albumin--cu(II)--amino acid ternary complex

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7 January 2021

Characterization of the copper(II)- and nickel(II)-transport site of human serum albumin. Studies of copper(II) and nickel(II) binding to peptide 1-24 of human serum albumin by 13C and 1H NMR spectroscopy

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7 January 2021

Circulating ceruloplasmin is an important source of copper for normal and malignant animal cells

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7 January 2021

Regulation of aortic CuZn-superoxide dismutase with copper. Caeruloplasmin and albumin re-activate and transfer copper to the enzyme in culture

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7 January 2021

Uptake of 67Cu by isolated human trophoblast cells

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7 January 2021

hCTR1: a human gene for copper uptake identified by complementation in yeast

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7 January 2021

The influence of amino acids on copper uptake by rat liver slices

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7 January 2021

Uptake of copper by mouse hepatocytes

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7 January 2021

Transport and intracellular distribution of copper in a human hepatoblastoma cell line, HepG2.

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7 January 2021

Copper accumulation and metabolism in primary monolayer cultures of rat liver parenchymal cells

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7 January 2021

Copper(I) transfer into metallothionein mediated by glutathione

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7 January 2021

Reconstitution of ceruloplasmin by the Cu(I)-glutathione complex. Evidence for a role of Mg2+ and ATP

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7 January 2021

Copper,zinc superoxide dismutase is primarily a cytosolic protein in human cells

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7 January 2021

Secretion of lysyl oxidase by cultured human skin fibroblasts and effects of monensin, nigericin, tunicamycin and colchicine

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7 January 2021

The lysosomal copper concentration in the liver in primary biliary cirrhosis

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7 January 2021

Immunohistochemical demonstration of the cytoplasmic copper-associated protein in the liver in primary biliary cirrhosis: its identification as metallothionein

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7 January 2021

PROGRESSIVE LENTICULAR DEGENERATION: A FAMILIAL NERVOUS DISEASE ASSOCIATED WITH CIRRHOSIS OF THE LIVER

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https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

Wilson disease: genetic basis of copper toxicity and natural history

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

Oral zinc in Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

Expression, Purification, and Metal Binding Properties of the N-terminal Domain from the Wilson Disease Putative Copper-transporting ATPase (ATP7B)

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

N-terminal domains of human copper-transporting adenosine triphosphatases (the Wilson's and Menkes disease proteins) bind copper selectively in vivo and in vitro with stoichiometry of one copper per metal-binding repeat.

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2899%2900249-4

7 January 2021

10.1016/S0162-0134(99)00249-4

Identifiers

DOI

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1 July 2017

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